반응 #598920

ord-854266ef6fe9460eb8e062902c0e0f75

반응 방정식

O=C1C(=O)c2cc3cccc4ccc5ccc1c2c5c43
cyclopenta[cd]pyrene-3,4-dione
O=C(Cc1ccccc1)Cc1ccccc1
1,3-diphenylacetone
CCO.Cc1ccccc1
ethanol toluene
[K+].[OH-]
potassium hydroxide
O=c1c(-c2ccccc2)c2ccc3cccc4cc5c6ccc(-c7ccccc7)c6c1c5c2c34
9,11-diphenyl-10H-pentaleno[1,2,3-cd]pyren-10-one

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONAfter the completion of the dropwise addition
  2. 2
    workup.STIRRINGstirred for 1 hour
  3. 3
    온도cooled
  4. 4
    여과The resulting precipitate was filtered
  5. 5
    세척washed with water, ethanol, and isopropyl alcohol, in that order
  6. 6
    기타dried
  7. 7
    온도by heating under reduced pressure

실험 절차

Next, 3 g (11 mmol) of cyclopenta[cd]pyrene-3,4-dione and 2.3 g (11 mmol) of 1,3-diphenylacetone were added to 300 mL of an ethanol/toluene (10/1) solution. Under stirring, 52 mL of 6 N aqueous potassium hydroxide was added dropwise thereto. After the completion of the dropwise addition, the mixture was heated to 50° C., stirred for 1 hour, and cooled. The resulting precipitate was filtered, washed with water, ethanol, and isopropyl alcohol, in that order, and dried by heating under reduced pressure to give 2.85 g of 9,11-diphenyl-10H-pentaleno[1,2,3-cd]pyren-10-one as a black solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09099656B2uspto-grants-2015_08